Methods for analyzing DNA
    2.
    发明授权

    公开(公告)号:US10724082B2

    公开(公告)日:2020-07-28

    申请号:US15835697

    申请日:2017-12-08

    Inventor: Michael Samuels

    Abstract: The invention generally relates to methods for increasing the amount of DNA available for analysis when using partitioned samples and parallel processing. For example, double-stranded DNA can be dissociated into two single-stranded components, and the single strands partitioned into different droplets prior to analysis. The disclosed methods are useful for performing digital PCR analysis on samples where the target DNA is not in abundance, for example when the sample originates from a body fluid or an FFPE sample.

    DIGITAL ANALYSIS OF NUCLEIC ACID MODIFICATION

    公开(公告)号:US20240185950A1

    公开(公告)日:2024-06-06

    申请号:US18538076

    申请日:2023-12-13

    CPC classification number: G16B20/10 G16B20/00

    Abstract: In certain aspects, methods of the invention involve performing modification state specific enzymatic reaction of nucleic acid in a sample, determining a value associated with efficiency of the modification state specific enzymatic reaction based on a control, determining an amount of target nucleic acid in the sample, and normalizing the amount of target nucleic acid based on the efficiency value. Based on the normalized amount of target nucleic acid, the method further includes determining whether the normalized amount of target nucleic acid is indicative of a condition.

    Digital analysis of nucleic acid modification

    公开(公告)号:US11901041B2

    公开(公告)日:2024-02-13

    申请号:US14505974

    申请日:2014-10-03

    CPC classification number: G16B20/10 G16B20/00

    Abstract: In certain aspects, methods of the invention involve performing modification state specific enzymatic reaction of nucleic acid in a sample, determining a value associated with efficiency of the modification state specific enzymatic reaction based on a control, determining an amount of target nucleic acid in the sample, and normalizing the amount of target nucleic acid based on the efficiency value. Based on the normalized amount of target nucleic acid, the method further includes determining whether the normalized amount of target nucleic acid is indicative of a condition.

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